The Speak Foundation

Our Story

The Speak Foundation was founded in 2008 as the first patient-led organization for muscular dystrophy, inspired by Kathryn Bryant Knudson's vision to support individuals with limb girdle muscular dystrophy (LGMD) and other rare neuromuscular diseases. This foundation aims to provide hope and resources to improve the quality of life for those affected.

Impact

Through its initiatives, The Speak Foundation has created a supportive community for individuals living with LGMD, offering access to cutting-edge research, educational resources, and financial assistance through various grant programs.

Why Donate?

Your contributions to The Speak Foundation directly support vital programs that provide education, advocacy, and financial assistance to individuals affected by limb girdle muscular dystrophy.

Get Involved

Join the mission to empower the LGMD community. Donate cryptocurrency or cash today to help fund research initiatives, patient support networks, and grant programs that make a real difference in the lives of those living with this condition.